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Zen1600

Manufactured by Malvern Panalytical
Sourced in United States

The ZEN1600 is a particle size and zeta potential analyzer developed by Malvern Panalytical. It utilizes dynamic light scattering (DLS) and electrophoretic light scattering (ELS) techniques to measure the size and surface charge of particles in liquid dispersions.

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6 protocols using zen1600

1

Comprehensive Characterization of Photocatalyst

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The crystalline structure of the
photocatalyst was characterized with an X-ray diffractometer (MAC
Science, MXP18, Cu Kα). The morphology and crystalline structure
of the photocatalyst were observed with a high-resolution transmission
electron microscope (JEOL, JEM-3000F, 300 kV). The band gap of the
photocatalyst was determined with UV–vis spectroscopy (Hitachi,
U-2800). EDX spectroscopy (Oxford 6587, Oxford Instruments) was conducted
to determine the elemental composition of the photocatalyst. The size
distribution of the NC suspension was determined with dynamic light
scattering spectroscopy (Malvern ZEN1600), in which DI water was used
as the solvent. The PL spectra were recorded with a fluorescence spectrometer
(Hitachi F-4500). The cell images were observed and taken using an
inverted microscope (Olympus CKX41).
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2

Particle Size Measurement by Laser Diffractometry

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By laser diffractometry, particle size was measured using a nano-size particle analyzer (Zen 1600 Malvern USA) in the range between 0.6 and 6.0 μm, under such conditions such as having particle refractive index 1.590, particle absorption coefficient 0.01, water refractive index 1.33, viscosity—cP, Temperature-25 °C and general calculation model for irregular particles. About 10−15 measurement cycles of 10 s each were taken and the data obtained were averaged by the respective instrument preloaded software (DTS, version 5.00 from Malvern) [38 (link)].
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3

Comprehensive Characterization of PR-GO Nanosheets

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Particle size of the PR-GO nanosheets was measured by laser diffractometry using a nano size particle analyzer (Zen 1600 Malvern USA) in the range between 0.6 nm and 6.0 μm. Transmission Electron Microscopy was performed on a Tecnai G2 spirit Biotwin (FP 5018/40), operating at an accelerating voltage of 80 kV. XRD measurements of PR-GO was taken with a PW 3040/60 PANalytical X-ray diffractometer that operated at a voltage of 45 KV and current of 30 mA with Cu Kα radiation (λ 1.54443 Ǻ). The diffracted intensities were recorded from 35° to 90° 2θ angles. EDX analysis was carried out with a Hitachi S 3400N, Japan, to identify the elemental compositions of the particles. The polysaccharide (PS), GO and PR-GO, were all analysed by Fourier transform infrared (FTIR) spectroscopy (Shimadzu 8400S fourier transform infrared spectrophotometer). The system worked in a diffuse reflectance mode at a resolution of 4 cm-1 in KBr pellets. The scanning data were obtained from the average of 50 scans in the range of 4000 to 400 cm-1. Raman spectra was monitored using 1.96 eV (633 nm) line of a He Ne laser in HORIBA-JOBIN-YVON Lab RAM HR 800 instrument by placing the sample solution into a semi-micro stopper cuvette with an exposure time of 1 s.
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4

Multimodal Characterization of Advanced Materials

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A transmission electron microscope (TEM) graph was obtained from FEI Tecnai G2 F30. X-ray diffraction (XRD) was measured by Rigaku D/MAX-2250 V. The UV‒Vis absorption spectrum was measured by Shimadzu UV-3600 Plus. Inductively coupled plasma‒optical emission spectrometry (ICP‒OES) was measured by Agilent Technologies 5100. The electrochemical workstation was CHI660E. Confocal laser scanning microscopy was carried out on a Nikon A1+R-980. The fluorescence microplate system was TECAN SPARK. The fluorescence spectrometer was an Edinburgh Instruments FLS 980. Dynamic light scattering (DLS) was measured by a Malvern ZEN1600. Deionized (DI) water was obtained from ELGA CENTRA. The flow cytometer was a Beckman CytoFlex S. Radiation therapy was carried out by a Varian Clinac 21EX (Trilogy), which was applied in the clinic at Huadong Hospital affiliated with Fudan University. X-rays (6 MeV) were used for all experiments, and the dose rate was 5 Gy/min.
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5

Characterization of Gold Nanoparticles

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The formation of gold nanoparticles was confirmed by the UV-Vis spectrophotometer (Hitachi 330 spectrophotometer) at 1 nm resolution only after the color change. The size of the nanoparticles was first measured by laser diffractometer (Zen 1600 Malvern USA) and then by Atomic Force Microscopy (AFM) using Nanoscope® 111A Veeco Multimode, USA. The characterization was done in tapping mode (NP10) with a silicon probe over scan sizes of 10 µm. The morphology of the nanoparticles was confirmed by Transmission Electron Microscopy (FP 5018/40, Tecnol G2 Spirit Bio TWIN). The XRD spectra were recorded from 30° to 80° 2θ angles using X-ray diffractometer (Seifert XDAL 3000) with CuKα radiation operated at 45 kV and 30 mA. The FTIR (Fourier Transform Infrared) spectroscopy (Shimadzu FTIR 8400S) was used to obtain the information about the functional groups with which the nanoparticles were stabilized.
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6

Particle Size Analysis of α-Fe2O3 and RBCs

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This was employed to evaluate the size distribution and average particle size of the α-Fe2O3 and RBCs samples. The DLS was performed using a Malvern Instruments-ZEN1600 (Serial number: MAL 1084260, UK) in backscattering mode at an angle of 173 ℃ and was operated at 25 °C. The results obtained were presented as size distribution by the intensity with the average particle size.
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